ALLERGY RELIEF  10MG- loratadine tablet 
YYBA CORP

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YYBA - WELMATE - LORATADINE ALLERGY RELIEF TABLETS, 10 MG (73581-203)

Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

Uses

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away [1-800-222-1222]

Directions

adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours
children under 6 yesrs of age      ask a doctor
consumers with liver or kidney disease ask a doctor

Other information

Inactive ingredients

lactose monohydrate, magnesium stearate, pregelatinized starch (maize), sodium starch, glycolate.

Questions?

call toll-free 1-866-933-6337

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ALLERGY RELIEF   10MG
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73581-203
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize7mm
FlavorImprint Code L;39
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73581-203-01100 in 1 BOTTLE; Type 0: Not a Combination Product07/28/2021
2NDC:73581-203-36365 in 1 BOTTLE; Type 0: Not a Combination Product07/28/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20831407/28/2021
Labeler - YYBA CORP (006339772)

Revised: 4/2022
Document Id: dcb60baf-5949-5ea3-e053-2995a90af24c
Set id: 6103cf98-40b1-4d27-8eb7-6f6a06949730
Version: 5
Effective Time: 20220415
 
YYBA CORP